外用非甾体类抗炎药凝胶对大鼠炎症和痛觉过敏的影响

S. Padi, Minakshi Gupta, J. Kehal, A. Aggarwal, Neeraj Kumar, R. Marwaha
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引用次数: 5

摘要

通过抑制环氧化酶(COX)起作用的非甾体抗炎药(NSAIDs)的全身使用严重阻碍了胃和消化性溃疡。局部给药非甾体抗炎药具有避免胃溃疡和消化性溃疡的优点,并能将药物输送到炎症部位。没有研究比较含有不同非甾体抗炎药的凝胶制剂的药理学特征。因此,我们尝试研究NIZER凝胶(尼美舒利,一种优先的COX-2抑制剂,每100 mg凝胶1 mg)和VOVERAN凝胶(双氯芬酸钠,一种非选择性COX (COX-1/2)抑制剂,每100 mg凝胶1 mg)对大鼠角叉菜胶诱导的炎症和痛症的抗炎和镇痛作用。NIZER凝胶或VOVERAN凝胶在给药前30min局部应用100mg,对卡拉胶诱导的大鼠炎症有明显的抗炎和抗衰老作用,其中NIZER凝胶作用更显著。结果表明,含有选择性COX-2抑制剂的凝胶在减轻炎症和痛觉过敏方面优于非选择性COX-1/2抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Topical Gels Containing Non-Steroidal Anti-Inflammatory Drugs on Inflammation and Hyperalgesia in rats
The systemic use of non-steroidal anti-inflammatory drugs (NSAIDs) which act by inhibiting cyclooxygenase (COX) is severely hampered by gastric and peptic ulcers. The topical delivery of NSAIDs has the advantages of avoiding gastric and peptic ulcers and delivering the drug to the inflammation site. There are no studies that compared the pharmacological profile of gel formulations containing different NSAIDs. Therefore, attempt has been made to study the anti-inflammatory and antihyperalgesic effects of NIZER gel (nimesulide, a preferential COX-2 inhibitor, 1 mg per 100 mg gel) and VOVERAN Emulgel (diclofenac sodium, a nonselective COX (COX-1/2) inhibitor, 1 mg per 100 mg gel) in carrageenan-induced inflammation and hyperalgesia in rats. A 100 mg of NIZER gel or VOVERAN Emulgel when applied topically 30 min before inflammogen administration showed marked anti-inflammatory and antihyperlagesic effects against carrageenan-induced inflammation in rats with more significant effect was observed with NIZER gel. The results indicate that gels containing a preferential COX-2 inhibitor are better than a non-selective COX-1/2 inhibitor in alleviating inflammation and hyperalgesia.
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